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ArticleIndian dermatology online journal2026

Mucocutaneous Manifestations of Primary Systemic Amyloidosis: A Descriptive Study from Eastern India.

Sudip K Ghosh, Sharmistha Panja, Biswajit Majumder, Maloy Pramanik

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Article in Indian dermatology online journal, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Sudip K GhoshDepartment of Dermatology, Venereology, and Leprosy, R. G. Kar Medical College, Kolkata, West Bengal, India.ORCID 0000-0002-3977-0462
Sharmistha PanjaDepartment of Dermatology, Venereology, and Leprosy, R. G. Kar Medical College, Kolkata, West Bengal, India.
Biswajit MajumderDepartment of Cardiology, R. G. Kar Medical College, Kolkata, West Bengal, India.
Maloy PramanikDepartment of Dermatology, Venereology, and Leprosy, R. G. Kar Medical College, Kolkata, West Bengal, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionPrimary systemic amyloidosis (PSA), also referred to as amyloid light-chain (AL) amyloidosis, is characterized by the deposition of insoluble monoclonal immunoglobulin light chains or L-chain fragments in a variety of tissues and organs of the body. There is a dearth of literature regarding the mucocutaneous manifestations of PSA in the Indian population, which prompted us to undertake the present study. AIM AND

objectiveWe aimed to study the clinical characteristics of mucocutaneous manifestations in patients with PSA at a tertiary care center in Kolkata. PATIENTS AND

methodsConsecutive patients with PSA, who presented to our facility with cutaneous features were included in this cross-sectional observational study done over 4 years.

resultsThe study involved 14 patients diagnosed with systemic amyloidosis (PSA) presenting with mucocutaneous symptoms. The mean age at diagnosis was 62.8 years, with a female-to-male ratio of 2:5. Myeloma-associated primary amyloidosis was identified in 35.7%. All patients showed pinch purpura, macroglossia, and tongue ridging. Periorbital purpura was seen in 92.8%, facial purpura in 85.7%, waxy nodules in 78.5%, xerosis in 57%, and diffuse alopecia in 35.7%. Relatively rare features included thickened skin, nail dystrophy, bullous lesions, lingual and subcutaneous nodules, atrophie blanche, and cutis laxa. Macular/lichen amyloidosis was also observed in one patient each. The head and neck were universally involved (100%). Eight patients had systemic features. LIMITATIONS: The study was limited by its hospital-based design, small sample size, and lack of lesional biopsies.

conclusionsPSA has a wide gamut of cutaneous features, and recognizing these skin lesions in the setting of PSA may be a significant clinical indicator of the underlying systemic illness.

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PMID42085007
PMCPMC13198804

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